RS61734479 FBLN5

Health Risk Chr 14:91936950
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What This Variant Does
"CLNSIG=5
Associated Conditions
Macular degeneration
age-related
3
Cutis laxa
Charcot-Marie-Tooth disease
demyelinating
IIA 1H
FBLN5-related disorder
autosomal dominant 2
autosomal recessive
type 1A
Macular degeneration
age-related
3
Cutis laxa
Other Variants in FBLN5
rs28939370 rs121434301 rs28939072 rs121434302 rs80338767 rs80338765 rs80338766 rs864309526 rs144288844 rs200178859
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